CA1259973A - Closed hemapheresis system and method - Google Patents

Closed hemapheresis system and method

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Publication number
CA1259973A
CA1259973A CA000489296A CA489296A CA1259973A CA 1259973 A CA1259973 A CA 1259973A CA 000489296 A CA000489296 A CA 000489296A CA 489296 A CA489296 A CA 489296A CA 1259973 A CA1259973 A CA 1259973A
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CA
Canada
Prior art keywords
rotor
housing
gap
outlet port
central
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
CA000489296A
Other languages
French (fr)
Inventor
William F. Mclaughlin
Donald W. Schoendorfer
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Individual
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Individual
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Publication of CA1259973A publication Critical patent/CA1259973A/en
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Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B04CENTRIFUGAL APPARATUS OR MACHINES FOR CARRYING-OUT PHYSICAL OR CHEMICAL PROCESSES
    • B04BCENTRIFUGES
    • B04B5/00Other centrifuges
    • B04B5/04Radial chamber apparatus for separating predominantly liquid mixtures, e.g. butyrometers
    • B04B5/0442Radial chamber apparatus for separating predominantly liquid mixtures, e.g. butyrometers with means for adding or withdrawing liquid substances during the centrifugation, e.g. continuous centrifugation
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M1/00Suction or pumping devices for medical purposes; Devices for carrying-off, for treatment of, or for carrying-over, body-liquids; Drainage systems
    • A61M1/14Dialysis systems; Artificial kidneys; Blood oxygenators ; Reciprocating systems for treatment of body fluids, e.g. single needle systems for hemofiltration or pheresis
    • A61M1/16Dialysis systems; Artificial kidneys; Blood oxygenators ; Reciprocating systems for treatment of body fluids, e.g. single needle systems for hemofiltration or pheresis with membranes
    • A61M1/26Dialysis systems; Artificial kidneys; Blood oxygenators ; Reciprocating systems for treatment of body fluids, e.g. single needle systems for hemofiltration or pheresis with membranes and internal elements which are moving
    • A61M1/262Dialysis systems; Artificial kidneys; Blood oxygenators ; Reciprocating systems for treatment of body fluids, e.g. single needle systems for hemofiltration or pheresis with membranes and internal elements which are moving rotating
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M1/00Suction or pumping devices for medical purposes; Devices for carrying-off, for treatment of, or for carrying-over, body-liquids; Drainage systems
    • A61M1/34Filtering material out of the blood by passing it through a membrane, i.e. hemofiltration or diafiltration
    • A61M1/3496Plasmapheresis; Leucopheresis; Lymphopheresis
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M1/00Suction or pumping devices for medical purposes; Devices for carrying-off, for treatment of, or for carrying-over, body-liquids; Drainage systems
    • A61M1/36Other treatment of blood in a by-pass of the natural circulatory system, e.g. temperature adaptation, irradiation ; Extra-corporeal blood circuits
    • A61M1/3693Other treatment of blood in a by-pass of the natural circulatory system, e.g. temperature adaptation, irradiation ; Extra-corporeal blood circuits using separation based on different densities of components, e.g. centrifuging
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M1/00Suction or pumping devices for medical purposes; Devices for carrying-off, for treatment of, or for carrying-over, body-liquids; Drainage systems
    • A61M1/36Other treatment of blood in a by-pass of the natural circulatory system, e.g. temperature adaptation, irradiation ; Extra-corporeal blood circuits
    • A61M1/3693Other treatment of blood in a by-pass of the natural circulatory system, e.g. temperature adaptation, irradiation ; Extra-corporeal blood circuits using separation based on different densities of components, e.g. centrifuging
    • A61M1/3696Other treatment of blood in a by-pass of the natural circulatory system, e.g. temperature adaptation, irradiation ; Extra-corporeal blood circuits using separation based on different densities of components, e.g. centrifuging with means for adding or withdrawing liquid substances during the centrifugation, e.g. continuous centrifugation
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D61/00Processes of separation using semi-permeable membranes, e.g. dialysis, osmosis or ultrafiltration; Apparatus, accessories or auxiliary operations specially adapted therefor
    • B01D61/02Reverse osmosis; Hyperfiltration ; Nanofiltration
    • B01D61/08Apparatus therefor
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D63/00Apparatus in general for separation processes using semi-permeable membranes
    • B01D63/06Tubular membrane modules
    • B01D63/062Tubular membrane modules with membranes on a surface of a support tube
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D63/00Apparatus in general for separation processes using semi-permeable membranes
    • B01D63/16Rotary, reciprocated or vibrated modules
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D69/00Semi-permeable membranes for separation processes or apparatus characterised by their form, structure or properties; Manufacturing processes specially adapted therefor
    • B01D69/04Tubular membranes
    • B01D69/043Tubular membranes characterised by the tube diameter
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2315/00Details relating to the membrane module operation
    • B01D2315/02Rotation or turning
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B04CENTRIFUGAL APPARATUS OR MACHINES FOR CARRYING-OUT PHYSICAL OR CHEMICAL PROCESSES
    • B04BCENTRIFUGES
    • B04B5/00Other centrifuges
    • B04B5/04Radial chamber apparatus for separating predominantly liquid mixtures, e.g. butyrometers
    • B04B5/0442Radial chamber apparatus for separating predominantly liquid mixtures, e.g. butyrometers with means for adding or withdrawing liquid substances during the centrifugation, e.g. continuous centrifugation
    • B04B2005/0464Radial chamber apparatus for separating predominantly liquid mixtures, e.g. butyrometers with means for adding or withdrawing liquid substances during the centrifugation, e.g. continuous centrifugation with hollow or massive core in centrifuge bowl
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B04CENTRIFUGAL APPARATUS OR MACHINES FOR CARRYING-OUT PHYSICAL OR CHEMICAL PROCESSES
    • B04BCENTRIFUGES
    • B04B5/00Other centrifuges
    • B04B5/04Radial chamber apparatus for separating predominantly liquid mixtures, e.g. butyrometers
    • B04B5/0442Radial chamber apparatus for separating predominantly liquid mixtures, e.g. butyrometers with means for adding or withdrawing liquid substances during the centrifugation, e.g. continuous centrifugation
    • B04B2005/0471Radial chamber apparatus for separating predominantly liquid mixtures, e.g. butyrometers with means for adding or withdrawing liquid substances during the centrifugation, e.g. continuous centrifugation with additional elutriation separation of different particles

Abstract

Abstract of the Disclosure A hemapheresis system and method in accordance with the invention comprises a stationary closed housing concentric about a central axis and a feed system that moves blood upwardly from the housing lower end toward an outlet port adjacent a substantially closed upper end. Within the station-ary housing is a double walled rotor concentric with the housing and rotatable by magnetic means within the housing on sealed end bearings. The space between the rotor walls defines a centrifugation gap into which whole blood is passed and within which centrifugal separation takes place as the rotor is spun at a relatively low rate. Whole blood also seeks to flow upwardly in the space between the rotor and housing, but this path is arranged to have a substantially higher flow impedance, so that the preferential path is within the centrifugation gap. At the upper end of the rotor, lighter matter such as plasma rich in platelets passes continuously inwardly to a central lengthwise passageway leading to an outlet port coaxial with the central axis, while heavier central matter flows through apertures in the outer rotor wall to the upper outlet port. In one example the differential impedance is established by housing and rotor configurations which diverge outwardly with compound curvatures, and with the space between rotor and housing leading to a closed end.
In another example the housing-rotor space is of restricted cross section and an opposing flow of compatible fluid is introduced in an intermediate region of the flow path. These systems are biologically closed and permit continuous return of packed cells to a donor as plasma is collected.

Description

~Z5~73 CLOSED HEMAPHERESIS SYSTEM A~D METHOD
Background of the Invention This invention relates to the separation of one or more constituents of blood, and is more particularly directed to a closed system employing centrifugal force for separating different constituents from whole blood based on density or size, such as the separation of platelets and plasma from whole blood,and to themethodfor carrying outsuch separation.
Whole blood consists broadly speaking oE red blood cells, white blood cells, platelets and plasma. Hemapheresis, which is directed to the separation of one or more constituents of blood,encompasses the extraction ofmany differentconstit-uents in the present state of the art. Plasma, for example, is separated from whole blood taken from donors and stored, with the packed cell remainders from the blood being returned to the donors. Red blood cells are concentrated and stored or reused, sometimes being held in frozen state before reuse.
There are numerous therapeutic apheresis applica-tions under study in which, using temporary or permanent separation of blood constituents, treatments or procedures are applied with sometimes dramatic benefit in amelioration of specific diseases or aEflictions. Itis sometimes desirable to separate leukocytes (white cells) from the red blood cells.
In other instances it is sought to extract platelets, which have a principal role in the clotting function, from red blood cells, Wit}l or without plasma. In all of these applications, the fragile blood tissue must be handled in a non-traumatic manner to avoid the introduction of hemolysis or the initiation of the clotting action.
Hemapheresis has heretofore principally been car-ried out using centrifugation techniques, or membrane ~5~73 filtration systems. Spinning whole blood in a centrifuge at an appropriately high rate separates constituents in accor-dance with their density, and by using a sufficiently high rateandanadequately long period of timea fine discrimination in constituents, in accordance with density, can be aehieved.
Batch centrifugation, however, is cumbersome and lenythy and not suitable for many applications in which it is desired to extract more than one constituent or return packed cells or other constituents to a donor.
Accordingly, cell separators have been developed and are in use, such as the Model 30 oEfered by Haemonetics Corp. ~or cell extraction. Thls includes a di.sposable unit comprising a rotatable rotor with an interior core so configured that heavier matter moves to the outside diameter oE the rotor/core combination, causing lighter matter to pass throuqh interior ports to an outlet. To achieve appropriate centrifugation Eorces so as to separate materials that are quite close in density requires high speed operation, and this device must be run for a substantial period of time before separation occurs. The Haemonetics unit accordingly is driven at approximately 4800 rpm and is quite expensive (in the range of $45.00 per unit) for a disposable device.
The great majority of such hemapheresis units are disposables that are used only once, because of the likelihood of transmission of infectious agents from one donor to another.
Furthermore the~Haemonetics device is regarded as an open path configuration, in that the inlet and outlet paths for theconstituentscan communicatewith theexterior environ-ment through rotary seals. Mierobe infiltration is a danger with such open systems, in consequence oE which the FDA
requires that the extracted matter be used within 24 hours to avoid the possibility of contamination.
Membrane filtration using a spinning rotor within a concentric shell has now been shown to be extremely efEective for separating some constituents of blood from others, as for example separation of plasma from leukocytes, platelets and red blood cells. There is a substantial di~ference in density and in the size of the elemental plasma which passes through 7~

the membrane relative to the cellular matter which is not filtered. However, when it is desired to separate certain cellular matter from other cellular matter, sizes may vary but little, as in the case with platelets which are of only slightly lower density in comparison to red blood cells. Membrane filtra-tion does not appear to be appropriate for performing -this function. Yet Eor certain applications it is of importance to extrac-t platelets separately, and for others to provide a plate-let rich plasma.
~here is therefore a widespread need for a closed system and method that will separate different constituents o:E
whole blood that are di.fferentiable in density and size, but only in a minor degree, and to be able to do so with a relative-ly low cost disposable unit that is closed to the exterior environment. A further aim is to provide a closed system and method for the separation of platelet rich plasma from whole blood.
Summary of the Invention According to a first aspect of the invention there is provided a system for extracting a platelet containing concen-tration from whole blood comprising in combination: a closedcell centrifugal separator having a central axis and including a housing having a fixed inlet port coupled to receive whole blood, a fixed packed cell outlet port spaced apart from the inlet port and a platelet rich plasma outlet port coaxial with the central axis, the centrifugal separator comprising rotatable rotor means within the housing r the rotor means being spaced apart from the housing and having a pair of concentric walls defining an internal centrifugation volume for continuously separating platelet rich plasma from heavier cell matter, means including aperture means in the rotor means for conducting whole blood into the centrifugation volume from the inlet port, means Eor conducting platelet rich plasma from the centrifuga-tion volume to the plasma outle-t port/ and means including second aperture means in the rotor means for conducting packed cells from the centriEugation volume to t:he packed cell outlet port;
means for rotating the rotor means within the housing without mechanical connection through the housing; and wherein the system further includes means establishing a lower flow impedance to blood flow in the centrifugation volume than in the spacing between -the rotor means and housing inner wall.
According to a second aspect of the invention there is provided a system for extracting lighter mat-ter from a liquid suspension, comprising: a closed cell centrifugal separator comprising a fixed housing concentric with a central axis and having a fixed inlet port coupled to receive the liquid suspension, a fixed outlet port spaced apart along the axis from the inlet port, and a coaxial outlet port for the lighter matter, the centrifugal separator comprising rotating interior double shell rotor means within the housing having a centrifugation gap, the rotor being spaced by a flow gap from the housing and including spaced apart aperture means in the outer shell provid-ing communication between the centrifugation gap and the ports in the housing; means coupled to the rotor means for rotating the rotor means without mechanical connection through the separator; and wherein the flow of liquid suspension is relative-ly unrestricted in the centrifugation gap in comparison to the flow gap.
According to a third aspect of the inven-tion there is provided a system for extracting platelets from whole blood comprising in combination: a closed cell centrifugal separator having an inlet port coupled to receive whole blood, a packed cell outlet port and a platelet rich plasma outlet port, the centrifugal separator comprising rotatable interior double shell ~.

- s -ro-tor means for continuously extracting platelet rich plasma from heavier cell matter and means deEining an interior centri-fugation gap and aperture means for directing whole blood from the inlet port into -the centrifugation gap and providing plate-let rich plasma to the plasma outle-t port from the centrifugat:ion gap; and rotatable plasmapheresis means including a central spinner within an outer housing, means for feeding platelet rich plasma Erom said centrifugal separator -to said plasmapheresis means, said plasmapheresis means further including a membrane on at least one of the surfaces oE the spinner or housing for extracting plasma, and outlet means for platelets not passing through the membrane.
According to a fourth aspect of the invention there is provi.ded the method of centrifuging separating constituents of blood with a stationary housing and internal rotor system and without exposure to the environment comprising the steps of: feeding whole blood into a limited substantially stationary first volume having a fixed outer periphery defined by the stationary housing and an inner periphery defined by the inter-nal rotor system, -the first volume being concentric about a central axis; feeding the whole blood from said first volume into a concentric rotating second volume that is defined by the rotor system within the first volume; passing heavier matter in the whole blood from the second volume through the first volume in one region; passing lighter matter in the whole blood from the second volume along the central axis through the first volume in a second region; and rotating the rotor system without mechan-ical connection through the housing.
According to a fifth aspect of the invention there is provided a system for continuously centrifugally separating lighter constituents of whole blood into packed cells and plasma fractions, comprising: a stationary housing having an in-terior -Sa-cavity defined principally by an inner wall concentric about a central axis and including a whole blood input port adjacent a first end thereof and a packed cell ou-tlet port adjacen-t the second end thereof; rotor means disposed and rotatable within the interior cavity of the housing, the rotor means including spaced apart outer and inner walls concentric about the central axis, the outer wall being spaced apart from -the inner housing wall and includiny first aperture means adjacent the first end thereof for passing blood to be centrifugally separated into the space between the outer wall and the inner wall, the rotor means further including means defining a radial inward path from the space between the outer and inner walls to the central axis at the second end thereof, and a central passageway communicat-ing with the radial inward path and concentric with the central axis, and the rotor means further including second aperture means in the outer wall at the second end thereof; means coupled to -the rotor means for rotating the rotor means at centrifuga-tion speed within the housing; plasma outlet port means in the hous-ing in communication with the central passageway in the rotor means; means disposed along the spacing between the outer wall of the rotor means and the inner wall of the housing for restrict-ing passage between the rotor means and housing of the whole blood fed into the inlet port in relation to passage of blood in the space between the rotor outer wall and inner wall; and wherein the residence time of the blood passing in the centrifu-gation gap between the inner and outer walls of the rotor means is sufficient rela-tive to the rota-tional speed -to provide a radial gradient between packed cells at the outer radius and platelet rich plasma at inner radii, at the second end thereof, such that packed cells move continuously through the second aperture means in the rotor means and pla-telet rich plasma moves continuously inwardly to the central passageway.

~S~973 -5b-According to a sixth aspect of -the invention there is provided a system for continuously centrifugally separating platelet rich plasma from cellular matter as whole blood is fed in, comprising: double wall rotor means concentric with the vertical axis and the walls defining a vertically ascending centrifugation gap about a central axis, the rotor means inc]ud-ing a central passageway concentric with the central axis and means providing a radially inward path from the uppex region of the centrifuga-tion gap to the central passageway, the rotor means further including, at the upper end thereof, means for permitting ou-tward flow from the rotor of heavier matter as lighterweight matter moves radially inward to the central pass-ageway; housing means disposed substantially concentrically about the rotor means and including a sealed inlet port for in-put blood adjacent the bottom end of the rotor means, a sealed outlet port for heavier constituents adjacent the upper end of the rotor means, and a sealed outlet port for separated lighter constituents adjacent the lower end of the rotor means and in communication with the central passageway therein; means for rotating the rotor means within the housing without external mechanical connection through the housing, at centrifugation speed; means in the rotor means for communica-ting input blood in the lower region of the housing into the centrifugation gap;
and means associa-ted wi.th -the outer wall of the rotor means and the housing for providing a differential flow impedance between the centrifugation gap and the spacing between the rotor means and the housing, such as to facilitate upward ascension of blood constituents in the centrifugation gap.
According to a seventh aspect of the invention there is provided a continuous centrifugation system that is biologically closed and separates lighter from heavier fractions of a liquid input suspension, comprising: a stationary housing having a sub--5c-stantially cylindrical cavity disposed about a vertical central axis; the housing including a liquid suspension inle-t port adjacent a first end thereof and a heavier fraction outlet port adjacent the second end thereof; rotor means rotatably mounted within the housing and having spaced apart inner and outer right circular cylindrical walls defining a centrifugation gap between the first and second ends, the rotor means including first aper-ture means in the outer wall adjacent the first end providing inlet Elow into the centrifugation gap and second aperture mcans in the second end of the outer wall thereof providing outlet flow of heavier fractions; the system including means disposed along at least the mi.d region of the gap between the outer wall of -the rotor and the housing for impeding flow of the liquid suspension between the first and second ends; means coupled to the rotor means for rotating the rotor means within the housing at centrifugation speeds; and the rotor means further including means providing central passageway means for lighter fractions moving radially inwardly from the second end of the centrifuga-tion gap along the central axis o:E the rotor means and an outlet port for lighter fractions coupled to the housing and in communi-cation with the central passageway means in the rotor means.
According to an eighth aspect of the invention there is provided a system for centrifugal separation of selected constituents of blood without exposure of such constituents to external environment, comprising: a stationary housing having an outwardly diverging perimeter extending upwardly from a base portion containing an inlet port and a lower central outlet port, said housing including an upper central outlet port, said lower and upper outlet ports being disposed along the central axis of said housing, and upper and lower end bearings mounted on said central axis adjacent said upper and lower outlet ports, respec-tively, and including central apertures in said end bearings in -5d-communication wi-th said upper and lower ou-tlet ports, and a substan-tially :Elat upper end cap c].osing the upper portion of -the housing; a ro-tor having an exterior periphery generally con-forming to the periphery of -the housing but smaller than said housing and positioned therein to :Eorm a first predeterrnined gap between said rotor and said housing, means mounting said rotor for rotation on -the upper and lower end bearinys and including a flat upper end cap closing the upper portion oE the ro-tor at the periphery of greatest diameter thereof, an upper conduit in said end cap communicatiny between the interior of -the rotor at the outer periphery of greatest diameter, the central aperture in said upper end beariny and the upper outlet port along the central axis, said rotor further including aper-tures in the base portion thereof communica-ting with said inlet port for feeding blood constituents into the interior of the rotor, and a deflector plate disposed in the region of greatest diameter of the rotor at the upper end thereof and disposed adjacent to and substantially parallel to the end cap thereof and defining a passage between the deflector plate and the end cap of the rotor communicating with the upper conduit, thereby to permit heavier matter in the blood constituents to pass from the interior of the rotor through the apertures in said def]ec-tor plate and through said last mentioned passage to the upper conduit; a core mounted within the rotor, the core having an exterior conEiguration generally conforming to the periphery of the rotor but smaller than said rotor and forming a second predetermined gap between the rotor and the core, the core hav-ing an upper portion spaced from said deflector plate and having a reentrant central conduit in communication with the aperture in said outer end bearing and means mounting said core for rotation on sai.d rotor, the core rotating with the rotor such that lighter matte:r in the blood constituents wi-thin the second ~3 gap in the interior of the rotor moves radially inwardly through the passage batween the upper portion of said core and said deflector plate, through the reentrant central conduit, the central aperture in said lower bearing and the lower output port, as heavier matter in the blood constituents in the second gap passes through the apertures in said deflector plate as aforesaid.
The invention further provides a centrifugal separator .system for extractlng lighter matter from a llquid suspension comprising: a housing having a central axis, an inlet port to said housing coupled to receive the liquid suspension, a heavier matter outlet port from said housing axially spaced ~rom the inlet port and a lighter matter outlet port from said housing; a rotating interior double shell rotor dispose~ within said housing for rotation about the central axis, said rotor including an outer shell and an inner shell and a centrifu~ation gap between said inner and outer shells, said rotor being spaced fxom said housing by a flow gap and including aperture means in said outer shell providing communication between the centrlfugation gap and said lnlet port and said heavier matter outlet port; a conduit within said doubla shell rotor for conducting the lighter matter from the centrifugation gap to said lighter matter outlet port, which is in fluid communication with said conduit; means within said housing, coupled to said rotor, for rotating said rotor wlthin said housing; and wherein the flow of liquid suspension i relatively unrestricted in the centrlfugation gap in comparison to the flow gap.
Th~ invention also provides a continuous flow centrifugal separator comprising: a fixed housing disposed about a central axis and having an inlet port, an outlet port 5e for heavier matter that is axially spaced from the lnlet port and an outlet port for lighter matter; and a rotor disposed within the housing for rotation about the central axis, the rotor having an outer ~hell and an inner wall spaced radially inward from the outer shell to def:Lne therebetween a gap which extends axially between the housing lnlet port and the housi.ng heavier matter outlet port, the gap being closed at each end, the outer shell having at least one shell inlet port ~herein axially disposed opposite the hous:Lng inlet port to provide communication of fluid from the housing inlet port to the gapr at least one shell heavier material outlet axially spaced from the shell inlet port in a direction toward the housing heavier material outlet port to provide communication from the gap to the housing heavier mater$al outlet port, the rotor defining a communication path for lighter material ~rom a position in the gap radially inward of the shell heavier material outlet port to the shell lighter materlal output port.

. 5~

Brief Descrlption oE the Drawings A better understanding of the invention may be had by reEerence tothe following description,taken inconjunction with the accompanying drawings, in which:
Fig. 1 is a perspective view, partially broken away, oE a closed system Eor centrifugal separation oE the constitu-ents oE blood;
Fig. 2 is a cross-sectional view oE the arrangement oE Fig. l;
~ig. 3 is a fragmentary view of a portion of the separator oE Figs. 1 and 2;
Fig. 4 is a block diagram representation ofa dispos-able systern Eor extraction of platelets from whole blood;
Fig. 5 is a side sectional view of a difEerent system Eor centrifugal separation of blood constituents;
Fig. 6 is a perspective view, partially broken away, of the sys~em of F`ig. 5;
Fig. 7 is an enlarged Eragmentary sectional view of -a portion oE the system of Figs. 5 and 6, showing the manner in which separation occurs; and Fig. 8 is a block diagram representation oE a system using the arrangement of ~igs. 5-7 for taking whole blood from a donor, returning certain fractions and collecting other certain Eractions.
Detailed Description o-E the Invention ~ hemapheresis system in accordance with the inven-tion, referring to Figs. 1 and 2 of the drawings, comprises a biologically closed cell separator 10 including a stationary outer housing 12, a rotor outer wall 14, and a rotor core or inner wall 16 positioned within the rotor and defining witll the rotor a double shell system. These elements are mounted concentric with a central vertical axis, the vertical disposi-tion being referred to Eor convenience and ease of description in the specification and claimsO lt will be appreciated from the following description, however, that these systems do not require a particular orientation or gravitational effect and can be used in diEEerent juxtaposition than the true vertical.
The space between the rotor wall 14 and core 16 defines a ~5~

shaped centrifuging chamber that presents a lower impedance to flow than does the space between the rotor ~alL 14 and the housing 12. The housing 12 has a relatively narrow base portion 18 and an upwardly and outwardly diverging portion or bowl 20 whichextends from the base to a ~inal, substantially vertical section. The base portion 18 oE the housing has an inlet por~ 21 and a lower central outlet port 24 positioned adjacent to each other along the central axis of the housing.
The upper end of the housing is closed by an upper housing cap 26 connected across the end of the upwardly divergent bowl 20 of the housing. The housing cap 26 includes an upwardly extending boss at its mid region to ~orm an upper central housing portion 2~ which terminates in an upper outlet port 30 which also extends along and is coaxial with the central axis of the housing 12.
The rotor wall 14 has an exterior shape generally conforming to the periphery of the outer housing 12, and includes a lower, necked down, base portion 32 and an outwardly and upwardly curved portion 34 oE double curvature forming a rotor bowl, the upper end of the rotor being closed on the outside by a hori~ontal rotor cap 36. The rotor wall 14 is spaced apart from the inner wall of the housing 12 to form an adequate clearance gap to receive a predetermined inlet volume of blood that is confined principally to the lower part of the space between the housing 23 and the rotor 14.
Blood flowing upwardly in this space is substantially non-rotating because of the stationary housing 12 wall and in addition acts against gas trapped in the closed upper end of the rotor-housing gap, which gas acts as a compliance opposing increased upward advance of the inlet whole blood in this space. Thus in the rotor-housing gap the blood rises only to a certain level below the upper portion of the housing.
The rotor cap 36 is Eormed with an upwardly extending c~entral conduit 40 positioned along the central axis of the housing and the rotor, and communicating between the interior of the hollow rotor from the outer periphery oE greatest diameter, and the upper outlet port 30 of the housing.

~D~

The rotor wall 14 is coupled to and is r,otatable on upper and lower end bearings 42 and 44, respectively, that are coaxial with the central axis. The upper beariny 42 comprises a stationary stainless steel pivot pin having a central orifice and mounted as by a press Eit in the upper outlet port 30 on the central,housing portion 28. A compliant O-ring 48 is captured between the rotatable central conduit 40 at the upper end oE the rotor and the lower end oE the pivot pin, to Eorm an upper fluid and pressure seal between the rotor and'the stationary housing. The lower bearing 44 comprises a stationary stainless steel pivot pin having a , central orifice, fixed as by a press Eit to the inner wall of the lower central outlet port 24. ~n o-ring 52 is retained in a groove 53 formed on an upstanding central tubular portion 54 mounted on the base portion 32 o~ the rotor. The O-ring 52 makes slidable contact with the outer surEace of the pivot in the oriEice oE the pin 44,and can shift slightl~ up and down the pivot pin in response to any limited axial motion oE
the rotor, and maintain a fluid and pressure seal between the rotor and the outer housing wall. Leakage across the seal can only take place within the interior oE the housing so that the flow paths are isolated Erom exterior contamination.
The lower end oE the central tubular portion 54 has a shoulder 55 which contacts the upper end of pivot pin 44 to-support tlle rotor wall 14.
The base of the central tubular member 54 on the rotor includes a plurality of apertures 56 spaced circumfer-entially around the member 54 about the pivot pin 44. The rotor 14 also includes an upper deflector plate 58 positioned just below the rotor cap 36, and connected across the upper end of the rotor in the region of greatest diameter thereof.
The deflector plate 58 has a plurality of apertures 60 spaced circumferentially around the outer diameter oE the plate near the outer periphery~ and permitting flow into an upper chamber between the cap 36 and the deflector plate 58.
The rotor core 16 is mounted concentrically within the interior of the hollow rotor wall 14 to rotate as part of the rotor structure. The exterior conEiguration oE the core 16 conforms to but is spaced apart from the rotor wall 14 so that the centriEugation volume has an increasing radii o~
curvature as one proceeds in the upward direction. The rate of change of the radius of curvature, however, is not constant.
The core 16 comprises a base portion 62 and an upwardly and outwardly divergent portion 64 oE bowl shape, a top portion 66 and a reentrant central conduit or passageway 68 connected to the base 62 and providing a flow path down from the top of the rotor. The central conduit 68 of the core includes a bottom portion 69 which is fitted around the central tubular portion 5~ of the rotor 14 str`ucture. The space between the outer wall of the core 16 and the rotor wall 14 therefore de~ines a second or centrifugation gap 70 through which the substantial majority of the volume oE liquid to be processed is conducted.
A cylindrical magnet 72 is mounted within the upper central housing 28 concentrically about the central vertical axls, and is fixed as by press fitting around the central conduit 40 at the upper end of the rotor 14. The magnet 72 when driven thus turns the rotor and the interior core within the upper and lower end bearings 42 and 44. ~n external magnetic-type rotary drive, indicated only generally at 74, is disposed about the housing 28 -to couple rnagnetically to the inner magnet 72 and provide synchronous rotation o~ the entire internal structure comprising the rotor wall 14 and core 16, without the requirement for any direct mechanical coupling.
The operation of the device oE Figs. 1 and 2 will be described hereafter in an application Eor the separation oE whole blood into packed cells and platelet rich plasma.
By packed cells is meant the combination of red blood cells and white blood cells, in the absence of platelets and plasma.
It will be understood, however, that this is only one example oE the application of the closed cell separator and method of the present invention, and other specific separation appli-cations can be carried out utilizing the invention system.
Referring to Figs. 1 and 2, the rotor 14 and core 16 are rotated by the external magnetic rotary drive 74, as whole blood enters within the stationary housing 12 through the whole blood inlet port 22. ~s the blood travels vertically upward into the housing interior it meets the bottom interior portion of the spinning rotor :L4 and Eills the gap 38 between the rotor and housing, rising to a predetermined height. This height is determined principally by the input pressure of the whole blood, the rotational velocity of the rotor, the rela-tionship between the centrifugation qap and the relatively staticrotor-housing gap, and the maximum radius of the centri-fugation gap, and the level of back pressure presented by thegas entrapped above the blood, in the closed end of the rotor-housing space. The whole blood also enters and fills a gap 76 between the lower stainless steel pivot pin 44 and the base portion 32 at the interior oE the tubular portion 54 of the l-o~or. The blood then passes through the ring of blood inlet apertures 56 into the lower end of the centrifugation gap 70 between the core 16 and the rotor wall 14. slood in the gap 38 between the housing 12 and rotor wall 14 rotates only at the rotor surface through viscous drag and therefore establishes a hydraulic pressure source when the operation stabilizes.
The blood is forced upwardly within the centriEu-gation gap 70 via the apertures 56 by the initial centrifugal forces imparted by viscous drag from the spinning rotor, the input pressure, and also by the compensating hydraulic head generated by the blood level in the outer gap 38. As the system continuously feeds blood into the housing at the inlet port 22, -the upward flow in the gap 70 between the core 16 and rotor wall 14 is continuous. As blood is impelled by centrifugal force and feed pressure, rotational velocity in-creases in the mid region where the radius arm of the centrifu-gation gap 70 increases. The outward surge of blood begins where the gap 70 turns outwardly, converting rotational energy of the rotor into upward movement which continues until the top portion of the rotor is reached. As previously noted, the rotor core 16 is designed to provide a low volume centrifu-gation gap 70 in the rotor, such as a volume of the order of about 50 ml.

As the whole blood moves upwardly from the inlet apertures 56 along the centri~ugation gap 70 within the rotor, the less dense plasma portion containing platelets concur-rently migrates toward the wa:Ll of the core 16 as the denser packed cells consisting of red and white blood cells are urged under the centrifugal forces to the outside of the gap 70.
The rotor is relatively large in diameter~ e.g. 4 to 5 inches, so that adequate centrifugal force can be generated at low rpm for this separation to occur by the time the deflector plate 58 is reached. With a rotor radius of 2.5 inch, at 2000 rpm there is a maximum of approximately 300 g Eor cell separa-tion. Theresidence time in the centrifugation gap is adequate Eor centrifugal separation of the desired constituents.
~ s shown more clearly in Fig. 3, when the whole blood being separated in the centriEugation gap 70 reaches the upper and outermost por-tion or corner of the separator volume, at 78, extraction of packed cells takes place. ~t this region the more dense packed cells are quite precisely separated ~rom the less dense plasma and platelets which are adjacent the inner wall of the centrifugation gap 70. Thus the packed cel~s pass through the circumferential ring of apertures 60 in the deflector plate 58 into the passage 81 between the deflector plate 58 and the rotor cap 36. The inlet flow pressure is adequate to urge the packed cells toward the center of the separator until they reach and pass through the upper central conduit 40, pivot pin 42 and the upper outlet port 30. From the outlet port 30 the packed cells are pumped out oE the separator by suitable pump means (not shown) or collected in a drainage bag by gravity feed.
The platelet rich plasma (plasma and platelets) at the core 16 wall passes inwardly through the passage 83 between the top 66 of the core and the deflector plate 58 of the rotor into the central reentrant conduit 63 within the rotor core under the feed pressure. Again, the inlet flow pressure is used to overcome centrifugal force in this region, although an outlet pump (not shown) can be used to assist. The continuous flow, here aided by gravity, moves the plasma and platelets downwardly through the interior of the central ~:~5~973 tubular portion 54, pivot pin 44, and the lower outlet port 24. The platelet rich plasma is then collected in an attached receptacle or pumped out of the separator by suitable means (not shown).
The diameter of the ring oE blood inlet apertures 56 on the rotor is kept small to enable a greater difEerential between the minimum and maximum centrifuging radii. The ratio of platelet rich plasma (PRP) to packed cells removed can be controlleclsomewhat by uslng pumps to extract one or the other outlet flows at speciEic rates.
~ An important feature of the cell separator of the invention is that the whole blood moves upwardly in the centrifugation gap 70 in the rotor with dynamic force and for a sufficient time to achieve separation before it reaches the top of the gap 70. ~t the upper and outer region 78 there is adequate gradation between the less dense platelet rich plasma portion and the denser packed cell portion, to effect the needed separation. The construction of the cell separator permi-ts separation of the light density material from the heavy density material by a gentle spinning of the rotor at relatively low speeds, e.g. 2000 rpm, as compared to the speed of rotation between 4000 and 5000 rpm of conventional cell separators.
The rotor, core and outer housing or shell of the cell separator all can be formed of plastic and the whole device isdisposableafter a single use. Hence, thecentrifugal separator device of the invention is of simple and economic construction.
The device of the present invention is particularly applicable to the separation of the components of blood. The chiefadvantage in this respect is that an effective separation of blood components can be obtained using a biologically closed system, as contrasted to currently employed open seal systems which are expensive. By "biologically closed" is generally meant, as witll the FDA requirements, that leakage through a gap between relatively moving parts is always in-ternal to the system. Such leakage can therefore only result in mixture of different constituents (such as plasma and 3~25~'73 packed cells) oE the whole blood itself. Exterior access is only possible at fixed ports providing inlet and outlet flows and these are much more assuredly sealed. While the device of the invention is oE particular applicability for the sepa-ration oE the packed cell pc~rtion from the platelet rich plasma portion of whole bloocl, it can also be employed ~or extracting other concentrates having medical interest, in~
cluding granulocytes, lymphocytes and neocytes, and can like-wise have application Eor cell washing and autotransfusion.
Fig. 4 illustrates another feature of the invention showing a disposable system which can harvest platelet concen-trate, pure plasma and packed cells. In this aspect of the invention a separator 10 as illustrated in Figs. 1 to 3 and described above is employed in conjunction with a membrane filtration unit 85 to provide continuous extraction of packed cells and plasma for return to a donor, while platelet concen-trate alone is separately collected.
In this system whole blood at 86 is fed to the cell separator 10, the packed cell output from the cell separator 10 is returned to the donor by a conduit 88 and the platelet rich plasma concentrate output Erom the cell separator, is fed via tubing 90 to the membrane filtration device 85.
Themembrane filtration devLce has an interior spin~
ner g2 within a stationary housing 91 and the outer wall of the spinner or the inner wall oE the housing has a membrane 93 covering a surEace thereof and an internal conduit system (not shown in detail) for collecting plasma passing through the membrane. In operation, the rotating action of the spinner keeps the input fluid sweeping the surface of the membrane, causing plasma to be transported through the membrane and into an outlet orifice 90. The plasma output at 90 can be harvested in a separate container at 95 and the platelet concentrate at 94 exiting the membralle filtration device can be collected in a container at 96.
If desired, the plasma at 90 can be returned at line 98 and through the packed cell return line at 88, to the donor. optionally, also, a fraction of the plasma can be introduced via line 100 with the whole blood Eeed at 86 to the cell .separator 10, to help elutrlate the platelets from the blood in the cell separator.
The membrane filtration unit at 85 in Figure 4 is described and claimed in Applicant's Canadian Patent Application No. 476,981 ~iled 20th ~arch 1985 entitled "Method and Apparatus For Separation Of Matter From Suspension".
Figures 5, 6 and 7 depict various aspects o~ a different biologically closed system for separatin~ lighter and heavier constituents from an input blood flow, this configuration being of even lower cos~ and more compact form.
Referring now to Figures 5-7, ~he housiny 110 for the sy~tem is configured generally as a right circular cylinder having a substantially right circular inner wall 112, a fixed inlet port 114 for blood input, e.g. whole blood, and a fixed outlet port 116 for outle~ of heavier fractions, adjacent the upper end thereof. At the bottom of the houslng 110 a ~ixed outlet port 118 for llghter blood fractions is dlsposed concentric with the central axis of the system. In the mid region along the vertical length of the housing 110, one or more fixed inlet ports 120 for a hiologically compatible fluid, such as plasma or saline solution, is disposed at one or more points about the periphery.
Within the housing 110 a double walled rotor 126 is concentrically disposed a`oout the central axis, and rotatably mounted in fixed upper and lower bearings 128, 130 respectively. The lower bearing 130 has a central orifice 132 in communication with the central outlet port 118 at the lower end of the housing, an internal rotary seal being provided by an 0-ring 134 about the bearing 130. At the upper end o~ the rotor 126, a magnetic element 136 is mounted so as to be externally driven by magnetic coupling from an external magnetic drive ~not shown in cletail inasmuch as it may be the same as shown in the example of Flgures 1--3). Other types of remote drives tha~ do not require mechanical connection through the housing may also be used, although it is preferred to employ the magnetic drive inasmuch as the intention ls to provide a low cost disposable. However, where other 14a ~3 considerations prevail, a completely diEferent configuration could be used while still providing a biologically closed system, as for example a completely self-contained battery driven motor or a motor with a power source that can be externally energized. In other instances, where continuous separation is desired but the systernneed not be biologically closed, an external drive directly coupled to the rator can be used.
q'he outer wall 140 oE the double walL rotor 126 comprises a modi~ied right circular cylinder, having a gap oE approximately 0.035" from the upper and lower portions of the inner wall 112 o~ the housing 110. However the outer walL includes an outwardly extending band 141 in its mid region that is spaced only about O.OlO" from the inner housing wall 112. The rotor inner wall 142 is concentric with the opposed base oftheouterwalll40 and provide~sacentriEugation gap 144 o~ approximately 0.010" to 0.075", here about 0.050"
Inlet apertures 146 about the lower region of the outer rotor wall provide an inletpath for input blood into the centrifuga-20 tiOIl gap region, while in the upper end of the outer wall 140outlet apertures 148 about the periphery are in communication with the outlet port 116 Eor the heavier fraction o~ the fractionated blood. At the upper end oE the rotor 126 a ilorizontal space defines a radially inward passageway 150 between the upper end 152 o~ the inner wall, which merges into a central passageway 154 extending along the central axis downwardly into communication with the central oriEice 132 -in the lower bearing 130, thus to define the internal core within the rotor 126. The horizontal upper end wall 156 oE
the outer wall 140 in this example merely serves as a closure for the internal passageways, and as a mechanical support for the magnetic element 136 and upper bearing 128.
In the system of Figs. 5-7, the rotor is driven at a suitable rotational velocity, e.g. 2000 rpm, and has a length, such as 4", adequate to provide a residence time within the centrifugation gap su~ficient to provide an ade-quate degree of continuous separation. To this end, whole blood or blood constituents containing both the heavier and ~Z~519~

lighter fraction passes through the inlet port to within the housing 110. The input blood flow attempts to movecontinuously upwardly toward the outwardly projecting band 141 on the outer wall 140 of the rotor 126, and through the inlet apertures 1~6 into the centri~ugation gap 1~4. The restricted gap between the stationary housing inner wall ll2 and the band l41on therotor126and the additional in~usion ofa compatible fluid introduce a substantial back pressure in this region.
Thus the preferential path for the inlet blood is within the centrifugation gap 144. ~s is evident to those skilled in the art, plasma derived in a process such as that depicted and described in conjunction with Fig. 4 may be used contin-uously as the compatible fluid input to the mid-region ports 120. Plas~a input in the mid region need not be high and the only e~fect is a slight reduction in the hematocrit of the packed cells provided from the outlet port 116.
Within the centriEugation gap 144, the upwardly ascending blood flow, under centrifugal Eorce, becomes in-creasingly radially separated into difEerent fractions. The neavier ~raction concentrates at the outer wall 140, and at ~ the uppermost region of the length of centrifugation gap 1~
heavier matter only is present at the outlet apertures 148.
The lighter fraction, specifically platelet rich plasma in the whole blood example, continuously moves inwardly along the radial passageway 150 toward the cen~tral axis. Selection of the total aperture area for the outlet apertures 148 relative to the input ~low rate enables a continuous balancing of the flows, and therefore continuous separation. The heavier fraction, such as cellular matter, combined with a small amount of bypass whole blood and plasma traverses the outer passageway across the outwardly projecting sur~ace 141. This flow is available for return to the donor, while the platelet rich plasma moves through the central passageway downwardly through the central orifice 132 and the lower bearing 130 and out thecentraloutletport118atthe bottomof thehousing 110.
The arrangement shown in Figs. 5 7 is particularly suitable for low cost, high volume applications. Unlike the usual centrifugation technique, it achieves high centrifugation efEiciency by establishing a relatively thin ~low path in which the radial mass that must be separated is small, so that cells can quickly migrate to the outside under relatively low radial velocities. The upwardly ascending flow is at a sufficiently slow rate Eor the flow to be essentially laminar, so that the centrifugation effects are not counteracted by turbulence, and a unieorm outer layer of helvy matter is made availabLe at the outl.et apertures in the rotor wall while the lighter fraction moves inwardly.
Consequently, radial ejection of the heavier fraction is automatic and smooth and the various geome-tries used in the prior centrifuge art, such as probes or separator edges, need not be employed to divide the fractions.
The system of Fig. 8 comprises an implementation of the device of Figs. 5-7, in which plasma and platelets are separated Erom whole blood taken from a donor (not shown) with the remaining fraction being returned to the donor. A
two needle system is used, a collection needle 160 and an input blood pump 162 feeding the blood input port 164 of a separator device 166 as described in conjunction with Figs. 5-7. Anticoagulant from a source 170 is also added to the input blood at a controlled rate by an anticoagulant pump 172(which along with the other pumps is depicted schematically as a conventional peristaltic device). The outlet port 174 for platelet rich plasma Erom the separator 166 feeds an input 176 of a platelet separator 178 of the rotating spinner type, as previously described, via a pump 180, with the plasma filtrate being collected in a bag or reservoir 182 and also a portion being shunted to an input port 183 in the mid region of the separator 166. The branched flow may be controlled by a valve or adjustable restrictor (not-shown) if desired, but positive pressure is maintained by a plasma return pump 18~.
Platelet concentrate from the platelet separator 178 is fed from the outlet port 186 for non-filtered remainder, as by gravity feed or a pump (not sKown) to a second collection bag 188.
As the separator 166 Eor platelet rich plasma func-tions, the packed cell output from the remaining outlet port 190 is fed by a return pump 192 to a return needle 194 at the donor, or, alternatively, to a third collection bag 196.
Contlnuous operation in this manner assures maintenance of the desired back pressure in the mid region o~ the separator 166, but it will also be understood that plasma 182 can be pumped from the plasma reservoir 182 itsel~ iE intermittent operation (e.g. a single needle system) is used.
The system of Fig. 8 is again a biologically closed, low cost, disposable system. The two ssparators 166, 178, lO three collection bags 182, 188, and 196, together with inter-connecting ELexible conduit, are all coupled together at static joinders only. Flow rates can be matched, as shown, Eor continuous operation but buffer reservoirs could be used as well.
From the Eoregoing, it is apparent that the present invention provides a method and system which is effective Eor the separation of blood components employing a closed com-pletely disposable system, as contrasted to currently employed open seal systems which are expensive.
Since various changes and modifications of the in-vention will occur to and can be made readily by those skilled in the art without departing from the invention concept, the invention is not to be taken as limited except by the scope of the appended clairns.

Claims (36)

THE EMBODIMENTS OF THE INVENTION IN WHICH AN EXCLUSIVE
PROPERTY OR PRIVILEGE IS CLAIMED ARE DEFINED AS FOLLOWS:
1. A system for extracting a platelet containing concen-tration from whole blood comprising in combination:
a closed cell centrifugal separator having a central axis and including a housing having a fixed inlet port coupled to receive whole blood, a fixed packed cell outlet port spaced apart from the inlet port and a platelet rich plasma outlet port coaxial with the central axis, the centrifugal separator compris-ing rotatable rotor means within the housing, the rotor means being spaced apart from the housing and having a pair of concen-tric walls defining an internal centrifugation volume for con-tinuously separating platelet rich plasma from heavier cell matter, means including aperture means in the rotor means for conducting whole blood into the centrifugation volume from the inlet port, means for conducting platelet rich plasma from the centrifugation volume to the plasma outlet port, and means including second aperture means in the rotor means for conducting packed cells from the centrifugation volume to the packed cell outlet port;
means for rotating the rotor means within the housing without mechanical connection through the housing; and wherein the system further includes means establishing a lower flow impedance to blood flow in the centrifugation volume than in the spacing between the rotor means and housing inner wall.
2. The invention as set forth in claim 1, wherein the rotor means is disposed to rotate about a vertical axis and wherein the inlet port is adjacent the lower end of the housing and the packed outlet port is adjacent the upper end of the housing, and wherein the means for rotating the rotor means com-prises a magnetic coupling drive.
3. The invention as set forth in claim 1 above, wherein the rotor means has an outer wall defining a surface of revolu-tion having a compound curvature including lower and upper sub-stantially vertical portions and an intermediate region widening radially outwardly.
4. The invention as set forth in claim 1 above, wherein the rotor means and housing inner wall are substantially right circular cylinders and include means for providing a restricted gap in the mid region thereof.
5. A system for extracting lighter matter from a liquid suspension, comprising:
a closed cell centrifugal separator comprising a fixed housing concentric with a central axis and having a fixed inlet port coupled to receive the liquid suspension, a fixed outlet port spaced apart along the axis from the inlet port, and a coaxial outlet port for the lighter matter, the centrifugal separator comprising rotating interior double shell rotor means within the housing having a centrifugation gap, the rotor being spaced by a flow gap from the housing and including spaced apart aperture means in the outer shell providing communication between the centrifugation gap and the ports in the housing;
means coupled to the rotor means for rotating the rotor means without mechanical connection through the separator; and wherein the flow of liquid suspension is relatively unrestricted in the centrifugation gap in comparison to the flow gap.
6. The invention as set forth in claim 5 above, wherein the plasma outlet port is at the bottom of the housing concen-tric with the central axis and the rotor means includes a cen-tral passageway in communication with said outlet port and means at the upper end thereof for conducting platelet rich plasma to the central passageway.
7. A system for extracting platelets from whole blood comprising in combination:
a closed cell centrifugal separator having an inlet port coupled to receive whole blood, a packed cell outlet port and a platelet rich plasma outlet port, the centrifugal separator comprising rotatable interior double shell rotor means for con-tinuously extracting platelet rich plasma from heavier cell matter and means defining an interior centrifugation gap and aperture means for directing whole blood from the inlet port into the centrifugation gap and providing platelet rich plasma to the plasma outlet port from the centrifugation gap; and rotatable plasmapheresis means including a central spinner within an outer housing, means for feeding platelet rich plasma from said centrifugal separator to said plasma-pheresis means, said plasmapheresis means further including a membrane on at least one of the surfaces of the spinner or housing for extracting plasma, and outlet means for platelets not passing through the membrane.
8. The invention as set forth in claim 7, further includ-ing means for receiving whole blood from a donor and supplying the whole blood to the separator and means for returning packed cells from the separator and plasma from the plasmapheresis means to the donor, and further including means for collecting the platelets from the plasmapheresis means.
9. The method of centrifuging separating constituents of blood with a stationary housing and internal rotor system and without exposure to the environment comprising the steps of:
feeding whole blood into a limited substantially stationary first volume having a fixed outer periphery defined by the stationary housing and an inner periphery defined by the internal rotor system, the first volume being concentric about a central axis;
feeding the whole blood from said first volume into a concentric rotating second volume that is defined by the rotor system within the first volume;
passing heavier matter in the whole blood from the second volume through the first volume in one region;
passing lighter matter in the whole blood from the second volume along the central axis through the first volume in a second region; and rotating the rotor system without mechanical connec-tion through the housing.
10. The method as set forth in claim 9, wherein the volumes are concentric about a central axis and including the steps of passing the whole blood upwardly from the lower regions of the first and second volumes to radially separate lighter from heavier constituents within the second volume, and selec-tively passing the lighter material laterally inwardly from the upper region of the second volume into the center of said second volume, and passing the heavier material from the upper region separately at the outer radius of the second volume.
11. A system for continuously centrifugally separating lighter constituents of whole blood into packed cells and plasma fractions, comprising:
a stationary housing having an interior cavity defined principally by an inner wall concentric about a central axis and including a whole blood input port adjacent a first end thereof and a packed cell outlet port adjacent the second end thereof;
rotor means disposed and rotatable within the interior cavity of the housing, the rotor means including spaced apart outer and inner walls concentric about the central axis, the outer wall being spaced apart from the inner housing wall and including first aperture means adjacent the first end thereof for passing blood to be centrifugally separated into the space between the outer wall and the inner wall, the rotor means further including means defining a radial inward path from the space between the outer and inner walls to the central axis at the second end thereof, and a central passageway communicating with the radial inward path and concentric with the central axis, and the rotor means further including second aperture means in the outer wall at the second end thereof;
means coupled to the rotor means for rotating the rotor means at centrifugation speed within the housing;
plasma outlet port means in the housing in communica-tion with the central passageway in the rotor means;
means disposed along the spacing between the outer wall of the rotor means and the inner wall of the housing for restricting passage between the rotor means and housing of the whole blood fed into the inlet port in relation to passage of blood in the space between the rotor outer wall and inner wall;
and wherein the residence time of the blood passing in the centrifugation gap between the inner and outer walls of the rotor means is sufficient relative to the rotational speed to provide a radial gradient between packed cells at the outer radius and platelet rich plasma at inner radii, at the second end thereof, such that packed cells move continuously through the second aperture means in the rotor means and platelet rich plasma moves continuously inwardly to the central passageway.
12. The invention as set forth in claim 11, wherein the system further comprises hollow bearing means disposed in the first region of the housing concentric with the central axis and with the central aperture thereof in communication with the central passageway of the rotor means, the bearing means at least partially supporting the rotor means and providing com-munication between the central passageway and the rotor means and the plasma outlet port means, and wherein the rotor means includes a magnetic structure coupled to one end thereof and the system further includes magnetic drive means disposed about the second end of the housing and magnetically coupled through the second end of the housing means to the magnetic means to rotate the rotor means and wherein rotary seal means are disposed between the rotor means and the housing to provide a biologically closed system.
13. The invention as set forth in claim 12, wherein the central axis is vertical and the means for restricting passage of the whole blood between the housing and rotor means comprises a compound curvature in the inner wall of the housing and an at least generally corresponding curvature in the rotor means, the compound curvature being along an ascending path providing an intermediate region of substantial radial expansion in the up-wardly ascending blood flow, between lower and upper regions of substantially vertical ascension, and further includes means closing the upper end of the space between the rotor means and housing.
14. The invention as set forth in claim 13, wherein the system includes upper and lower centrally apertured bearing means within the housing and rotatably supporting the rotor means, and wherein the packed cell outlet means is disposed about the central axis in communication with the interior of the upper end of the housing through the central orifice and the upper bearing means, and wherein the rotor means includes deflector plate means transverse to the central axis at the upper region of the rotor means and a central upper passageway above the deflector means and in communication with the packed cell outlet port means for providing a passageway for packed cells.
15. The invention as set forth in claim 11, wherein the housing inner wall and the rotor means comprise generally right circular cylindrical surfaces, and wherein the means for restricting passage of blood between the outer wall of the rotor means and the inner wall of the housing comprises means providing a restricted gap therebetween in the mid region of the system.
16. The invention as set forth in claim 15, wherein the system further includes means defining a fluid inlet port in the restricted gap region between the housing inner wall and the rotor outer wall, and means for feeding a fluid compatible with whole blood therein to provide a back pressure against whole blood seeking to move along the restricted gap.
17. The invention as set forth in claim 16, wherein the outlet port means for the packed cells is disposed in an upper region of the side wall of the housing and the whole blood input port is disposed in a lower region of the side wall of the housing.
18. A system for continuously centrifugally separating platelet rich plasma from cellular matter as whole blood is fed in, comprising:
double wall rotor means concentric with the vertical axis and the walls defining a vertically ascending centrifuga-tion gap about a central axis, the rotor means including a central passageway concentric with the central axis and means providing a radially inward path from the upper region of the centrifugation gap to the central passageway, the rotor means further including, at the upper end thereof, means for permitting outward flow from the rotor of heavier matter as lighterweight matter moves radially inward to the central passageway;
housing means disposed substantially concentrically about the rotor means and including a sealed inlet port for input blood adjacent the bottom end of the rotor means, a sealed outlet port for heavier constituents adjacent the upper end of the rotor means, and a sealed outlet port for separated lighter constituents adjacent the lower end of the rotor means and in communication with the central passageway therein;
means for rotating the rotor means within the housing without external mechanical connection through the housing, at centrifugation speed;
means in the rotor means for communicating input blood in the lower region of the housing into the centrifugation gap; and means associated with the outer wall of the rotor means and the housing for providing a differential flow impedance between the centrifugation gap and the spacing between the rotor means and the housing, such as to facilitate upward ascension of blood constituents in the centrifugation gap.
19. A continuous centrifugation system that is biological-ly closed and separates lighter from heavier fractions of a liquid input suspension, comprising:
a stationary housing having a substantially cylin-drical cavity disposed about a vertical central axis;
the housing including a liquid suspension inlet port adjacent a first end thereof and a heavier fraction outlet port adjacent the second end thereof;
rotor means rotatably mounted within the housing and having spaced apart inner and outer right circular cylindrical walls defining a centrifugation gap between the first and second ends, the rotor means including first aperture means in the outer wall adjacent the first end providing inlet flow into the centrifugation gap and second aperture means in the second end of the outer wall thereof providing outlet flow of heavier fractions;
the system including means disposed along at least the mid region of the gap between the outer wall of the rotor and the housing for impeding flow of the liquid suspension between the first and second ends;
means coupled to the rotor means for rotating the rotor means within the housing at centrifugation speeds; and the rotor means further including means providing central passageway means for lighter fractions moving radially inwardly from the second end of the centrifugation gap along the central axis of the rotor means and an outlet port for lighter fractions coupled to the housing and in communication with the central passageway means in the rotor means.
20. The system as set forth in claim 19, further including magnetic means coupled to the rotor means within the housing means, external drive means magnetically coupled to the magnetic means, for rotating the rotor means and core means within the housing means, and wherein the means for impeding flow comprises a substantially smaller gap between the rotor means and the housing than between the walls of the rotor.
21. A system for centrifugal separation of selected con-stituents of blood without exposure of such constituents to external environment, comprising:

a stationary housing having an outwardly diverging perimeter extending upwardly from a base portion containing an inlet port and a lower central outlet port, said housing includ-ing an upper central outlet port, said lower and upper outlet ports being disposed along the central axis of said housing, and upper and lower end bearings mounted on said central axis adjacent said upper and lower outlet ports, respectively, and including central apertures in said end bearings in communication with said upper and lower outlet ports, and a substantially flat upper end cap closing the upper portion of the housing;
a rotor having an exterior periphery generally con-forming to the periphery of the housing but smaller than said housing and positioned therein to form a first predetermined gap between said rotor and said housing, means mounting said rotor for rotation on the upper and lower end bearings and including a flat upper end cap closing the upper portion of the rotor at the periphery of greatest diameter thereof, an upper conduit in said end cap communicating between the interior of the rotor at the outer periphery of greatest diameter, the central aperture in said upper end bearing and the upper outlet port along the central axis, said rotor further including aper-tures in the base portion thereof communicating with said inlet port for feeding blood constituents into the interior of the rotor, and a deflector plate disposed in the region of greatest diameter of the rotor at the upper end thereof and disposed adjacent to and substantially parallel to the end cap thereof and defining a passage between the deflector plate and the end cap of the rotor communicating with the upper conduit, thereby to permit heavier matter in the blood constituents to pass from the interior of the rotor through the apertures in said deflec-tor plate and through said last mentioned passage to the upper conduit;

a core mounted within the rotor, the core having an exterior configuration generally conforming to the periphery of the rotor but smaller than said rotor and forming a second pre-determined gap between the rotor and the core, the core having an upper portion spaced from said deflector plate and having a reentrant central conduit in communication with the aperture in said outer end bearing and means mounting said core for rotation on said rotor, the core rotating with the rotor such that lighter matter in the blood constituents within the second gap in the interior of the rotor moves radially inwardly through the pass-plate, through the reentrant central conduit, the central aper-ture in said lower bearing and the lower output port, as heavier matter in the blood constituents in the second gap passes through the apertures in said deflector plate as aforesaid.
22. The system as set forth in claim 21, said means mounting said core for rotation on said rotor including an up-standing tubular central portion connected to the base portion of said rotor, the central conduit of said core being mounted on said tubular portion, and including first sealing means between the upper conduit on said rotor and the upper end bear-ing and second sealing means between the base portion of said rotor and said lower end bearing.
23. The system as set forth in claim 22, said sealing means comprises an O-ring positioned between said upper conduit and said end bearing, and said second sealing means comprising an O-ring mounted on the base portion of said rotor and in slidable contact with the lower end bearing, and means on the tubular portion of said rotor for limiting axial motion of said rotor, said upper and lower end bearings each comprising a stainless steel pivot pin.
24. The system as set forth in claim 23, said housing upper cap comprising a central housing portion, said outlet port being connected to the upper end of said housing portion, and including a magnet positioned in said upper housing portion and connected to the upper conduit of said rotor for driving same, said magnet rotating around said upper end bearing, and external drive means magnetically coupled to said magnet for rotating said magnet, and the rotor and core within the housing.
25. A centrifugal separator system for extracting lighter matter from a liquid suspension comprising:
a housing having a central axis, an inlet port to said housing coupled to receive the liquid suspension, a heavier matter outlet port from said housing axially spaced from the inlet port and a lighter matter outlet port from said housing;
a rotating interior double shell rotor disposed within said housing for rotation about the central axis, said rotor including an outer shell and an inner shell and a centrifugation gap between said inner and outer shells, said rotor being spaced from said housing by a flow gap and including aperture means in said outer shell providing communication between the centrifugation gap and said inlet port and said heavier matter outlet port;
a conduit within said double shell rotor for conducting the lighter matter from the centrifugation gap to said lighter matter outlet port, which is in fluid communication with said conduit;
means within said housing, coupled to said rotor, for rotating said rotor within said housing; and wherein the flow of liquid suspension is relatively unrestricted in the centrifugation gap in comparison to the flow gap.
26. A system in accordance with claim 25, wherein said rotating means coupled to said rotor means is adapted for rotating said rotor without mechanical connection thereto, from outside said housing.
27. A system in accordance with claim 25, wherein said housing is a biologically closed cell.
28. A system in accordance with claim 25, wherein the lighter matter can be expressed out of said lighter matter outlet port and the remainder of the liquid suspension can be expressed out of said heavier matter outlet port during rotation of said rotor means.
29. A system in accordance with claim 25, wherein said centrifugal separator is a continuous flow separator in which liquid suspension can be introduced into said housing through said inlet port, in which the lighter matter can be expressed out of said housing through said lighter matter outlet port, and in which the remainder of the liquid suspension can be expressed out of said housing through said heavier matter outlet port, all during rotation of said rotor means.
30. A system in accordance with claim 29, wherein said housing is a biologically closed cell.
31. A continuous flow centrifugal separator comprising:

a fixed housing disposed about a central axis and having an inlet port, an outlet port for heavier matter that is axially spaced from the inlet port and an outlet port for lighter matter; and a rotor disposed within the housing for rotation about the central axis, the rotor having an outer shell and an inner wall spaced radially inward from the outer shell to define therebetween a gap which extends axially between the housing inlet port and the housing heavier matter outlet port, the gap being closed at each end, the outer shell having at least one shell inlet port therein axially disposed opposite the housing inlet port to provide communication of fluid from the housing inlet port to the gap, at least one shell heavier material outlet axially spaced from the shell inlet port in a direction toward the housing heavier material outlet port to provide communication from the gap to the housing heavier material outlet port, the rotor defining a communication path for lighter material from a position in the gap radially inward of the shell heavier material outlet port to the shell lighter material output port.
32. A centrifugal separator according to claim 31, wherein the housing provides a biologically closed container.
33. A centrifugal separator according to claim 31, wherein the housing lighter material outlet port is concentric with the central axis.
34. A centrifugal separator according to claim 31, wherein a gap is defined between the rotor and the housing and at least a portion of the gap between the rotor and housing is no greater than the centrifugation gap.
35. A centrifugal separator according to claim 31, wherein at least a portion of the gap between the rotor and the housing is smaller than the centrifugation gap.
36. A centrifugal separator according to claim 31, wherein the centrifugation gap provides a flow path between the at least one shell inlet port and the at least one shell outlet port which is preferential to flow therebetween through a gap defined between the housing and the rotor.
CA000489296A 1984-08-24 1985-08-23 Closed hemapheresis system and method Expired CA1259973A (en)

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AU4726285A (en) 1986-03-24
JPH0536105B2 (en) 1993-05-28
EP0194271B1 (en) 1992-03-25
WO1986001426A1 (en) 1986-03-13
DE3585737D1 (en) 1992-04-30
US4911833A (en) 1990-03-27
EP0194271A1 (en) 1986-09-17
ATE74022T1 (en) 1992-04-15
NZ213160A (en) 1988-11-29
DE194271T1 (en) 1987-02-05
JPS62500011A (en) 1987-01-08
US4776964A (en) 1988-10-11
AU581458B2 (en) 1989-02-23
EP0194271A4 (en) 1988-09-07

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